S. Bellman

954 total citations
24 papers, 715 citations indexed

About

S. Bellman is a scholar working on Sensory Systems, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, S. Bellman has authored 24 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Sensory Systems, 6 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in S. Bellman's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (5 papers) and RNA regulation and disease (3 papers). S. Bellman is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Hearing Loss and Rehabilitation (5 papers) and RNA regulation and disease (3 papers). S. Bellman collaborates with scholars based in United Kingdom, Netherlands and Norway. S. Bellman's co-authors include Marcus Pembrey, Peter Phelps, William Reardon, S Malcolm, Maria Bitner‐Glindzicz, Christopher Wren, Svein Sörland, Jon Pritchard, Penelope Brock and Lisbeth Tranebjærg and has published in prestigious journals such as Human Molecular Genetics, European Journal of Cancer and Archives of Disease in Childhood.

In The Last Decade

S. Bellman

24 papers receiving 680 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
S. Bellman United Kingdom 12 317 307 165 161 119 24 715
Chongyu Ren United States 12 149 0.5× 237 0.8× 51 0.3× 79 0.5× 11 0.1× 14 470
K. Mees Germany 12 243 0.8× 83 0.3× 12 0.1× 38 0.2× 58 0.5× 64 593
Ann Marie Kazee United States 14 46 0.1× 191 0.6× 25 0.2× 70 0.4× 11 0.1× 21 691
Mitsuya Suzuki Japan 16 410 1.3× 125 0.4× 9 0.1× 134 0.8× 175 1.5× 77 818
Andres Veske Germany 11 71 0.2× 327 1.1× 14 0.1× 47 0.3× 15 0.1× 21 642
Krzysztof Morawski Poland 15 401 1.3× 60 0.2× 10 0.1× 277 1.7× 125 1.1× 83 715
Milan Profant Slovakia 12 156 0.5× 69 0.2× 16 0.1× 142 0.9× 229 1.9× 31 459
Denis Crimmins Australia 13 44 0.1× 395 1.3× 40 0.2× 39 0.2× 6 0.1× 28 700
T H Kirkham United Kingdom 18 55 0.2× 171 0.6× 7 0.0× 62 0.4× 25 0.2× 33 842
Neil S. Patel United States 11 111 0.4× 98 0.3× 7 0.0× 138 0.9× 53 0.4× 39 426

Countries citing papers authored by S. Bellman

Since Specialization
Citations

This map shows the geographic impact of S. Bellman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by S. Bellman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Bellman more than expected).

Fields of papers citing papers by S. Bellman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Bellman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by S. Bellman. The network helps show where S. Bellman may publish in the future.

Co-authorship network of co-authors of S. Bellman

This figure shows the co-authorship network connecting the top 25 collaborators of S. Bellman. A scholar is included among the top collaborators of S. Bellman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with S. Bellman. S. Bellman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
West, C, et al.. (2001). A study of the application of a frequency transposition hearing system in children. British Journal of Audiology. 35(1). 17–29. 9 indexed citations
2.
Blanton, Susan H., Maria Bitner‐Glindzicz, Arti Pandya, et al.. (2001). Haplotype analysis of the USH1D locus and genotype–phenotype correlations. Clinical Genetics. 60(1). 58–62. 17 indexed citations
3.
Papsin, B.C., C. M. Bailey, D. M. Albert, & S. Bellman. (1997). Surgical aspects of paediatric cochlear implantation. The Journal of Laryngology & Otology. 111(3). 240–244. 10 indexed citations
4.
Tyson, Jess, Lisbeth Tranebjærg, S. Bellman, et al.. (1997). IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome. Human Molecular Genetics. 6(12). 2179–2185. 233 indexed citations
5.
Papsin, B.C., C. M. Bailey, David Albert, & S. Bellman. (1996). Otitis media with effusion in paediatric cochlear implantees: the role of peri-implant grommet insertion. International Journal of Pediatric Otorhinolaryngology. 38(1). 13–19. 29 indexed citations
6.
Bellman, S.. (1996). Monitoring chemotherapy-induced hearing loss in children. European Journal of Cancer. 32(7). 1185–1188. 5 indexed citations
7.
Bellman, S., et al.. (1996). Evaluation of the E2L Toy Test as a screening procedure in clinical practice. British Journal of Audiology. 30(4). 286–296. 11 indexed citations
8.
Cohen, Mazal, Mary C. Francis, L. M. Luxon, et al.. (1996). Dips on Békésy or Audioscan Fail to Identify Carriers of Autosomal Recessive Non-Syndromic Hearing Loss. Acta Oto-Laryngologica. 116(4). 521–527. 6 indexed citations
9.
Bellman, S., A. Davies, Peter Fuggle, David Grant, & I Smith. (1996). Mild impairment of neuro-otological function in early treated congenital hypothyroidism.. Archives of Disease in Childhood. 74(3). 215–218. 39 indexed citations
10.
Bellman, S., et al.. (1994). Clinical applications of transcranial bone conduction attenuation in children. The Journal of Laryngology & Otology. 108(10). 834–836. 12 indexed citations
11.
Bellman, S.. (1992). Audiological medicine.. PubMed. 47(3). 205–6. 1 indexed citations
12.
Bellman, S., et al.. (1991). A new toy test to investigate the hearing status of young children who have English as a second language: A preliminary report. British Journal of Audiology. 25(5). 317–322. 2 indexed citations
13.
Phelps, Peter, et al.. (1991). X-linked deafness, stapes gushers and a distinctive defect of the inner ear. Neuroradiology. 33(4). 326–330. 155 indexed citations
14.
Reardon, William, Helen Middleton‐Price, Lodewijk A. Sandkuijl, et al.. (1991). A multipedigree linkage study of X-linked deafness: Linkage to Xq13-q21 and evidence for genetic heterogeneity. Genomics. 11(4). 885–894. 34 indexed citations
15.
Savage, Martin O., et al.. (1990). A new syndrome: hearing loss and familial salivary gland insensitivity to aldosterone in two brothers. The Journal of Laryngology & Otology. 104(12). 956–958. 6 indexed citations
16.
Bellman, S.. (1988). Screening for Hearing Impairment in Young Children. Archives of Disease in Childhood. 63(8). 1001–1001. 5 indexed citations
17.
Levitt, G., et al.. (1988). Outcome of preterm infants who suffered neonatal apnoeic attacks. Early Human Development. 16(2-3). 235–243. 24 indexed citations
18.
Brock, Penelope, Jon Pritchard, S. Bellman, & CR Pinkerton. (1988). Ototoxicity of high‐dose cis‐platinum in children. Medical and Pediatric Oncology. 16(5). 368–369. 33 indexed citations
19.
Stephens, Simon & S. Bellman. (1983). The prevention of hearing loss. International Rehabilitation Medicine. 5(2). 86–95. 2 indexed citations
20.
Bellman, S., et al.. (1964). CHEMOTHERAPY OF FIVE SUPRATENTORIAL MALIGNANT GLIOMAS WITH INTRA-ARTERIAL INFUSION OF METHOTREXATE.. PubMed. 127. 569–73. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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